Allele Registry

Canonical Allele Identifier: PA286921

Gene: ATM HGNC NCBI

ClinVar RCV:

RCV000115223

RCV000212038

RCV000457673

RCV001358622

RCV002288590

RCV003320457

ClinVar Variation:

127418

HGVS (amino-acid)	Matching Registered Transcripts
NP_000042.3:p.Arg2034Gln	CA286919 NM_000051.4:c.6101G>A